Colon Cancer: Gene >> SERPINF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254722
Start	1771086:1771086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341G>A
AA Mutation	p.Ser114Asn(p.S114N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254722
Start	1776597:1776597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852G>T
AA Mutation	p.Gln284His(p.Q284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254722
Start	1770029:1770029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Ala88Thr(p.A88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254722
Start	1772065:1772065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254722
Start	1775062:1775062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254722
Start	1777381:1777381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254722
Start	1771137:1771137(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.397delC
AA Mutation	p.Gln133ArgfsTer18(p.Q133Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254722
Start	1771969:1771969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537G>T
AA Mutation	p.Glu179Asp(p.E179D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254722
Start	1771883:1771883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451A>C
AA Mutation	p.Lys151Gln(p.K151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript